Department of Medical Oncology, Universitair Ziekenhuis Brussel (UZ Brussel)/Vrije Universiteit Brussel (VUB), Brussels, Belgium.
Department of Medical Oncology, Algemeen Ziekenhuis Sint-Lucas, Brugge, Belgium.
Pigment Cell Melanoma Res. 2024 Nov;37(6):822-830. doi: 10.1111/pcmr.13186. Epub 2024 Jul 11.
Leptomeningeal melanoma metastases (LMM) are associated with poor survival. Diagnosis is based on clinical presentation, brain MRI and cerebrospinal fluid (CSF) analysis. Inconclusive findings at initial presentation can delay treatment. In this single-center case series, detection of BRAF- and NRAS-mutant cell-free tumor DNA (cfDNA) in CSF was evaluated as a complementary diagnostic biomarker. In 12 patients with clinical suspicion of LMM, a retrospective analysis of MRI, CSF cytology and cfDNA analysis on 1 mL of CSF using the Idylla® platform was carried out. Nine patients displayed MRI abnormalities suggesting LMM. CSF analysis identified malignant cells in three patients (including one without MRI abnormalities). BRAF- or NRAS-mutant cfDNA was detected in CSF of nine patients (eight with and one without MRI abnormalities; all patients with positive CSF cytology). Subsequent follow-up confirmed LMM in all patients with positive and in one patient with a negative CSF cfDNA analysis (sensitivity 81.8%; specificity 100%). Our findings suggest that analyzing BRAF- and NRAS-mutant cfDNA in CSF using the Idylla® platform holds promise as a sensitive and specific complementary diagnostic biomarker for LMM, particularly in case of inconsistency between imaging and CSF cytology. The 110-min analysis can facilitate urgent treatment decisions.
脑脊膜黑色素瘤转移(LMM)与预后不良相关。诊断基于临床表现、脑部 MRI 和脑脊液(CSF)分析。初始表现不明确可能会延迟治疗。在这项单中心病例系列研究中,评估了 CSF 中 BRAF 和 NRAS 突变的无细胞肿瘤 DNA(cfDNA)作为辅助诊断生物标志物的作用。在 12 例临床疑似脑脊膜黑色素瘤的患者中,对 MRI、CSF 细胞学和使用 Idylla®平台对 1mL CSF 进行的 cfDNA 分析进行了回顾性分析。9 例患者显示出提示 LMM 的 MRI 异常。CSF 分析在 3 例患者中发现了恶性细胞(包括 1 例无 MRI 异常)。9 例患者的 CSF 中检测到 BRAF 或 NRAS 突变 cfDNA(8 例有 MRI 异常,1 例无 MRI 异常;所有阳性 CSF 细胞学患者)。后续随访证实所有 cfDNA 分析阳性患者和 1 例 cfDNA 分析阴性患者均存在 LMM(敏感性 81.8%;特异性 100%)。我们的研究结果表明,使用 Idylla®平台分析 CSF 中的 BRAF 和 NRAS 突变 cfDNA 具有作为 LMM 敏感且特异的辅助诊断生物标志物的潜力,特别是在影像学和 CSF 细胞学不一致的情况下。110 分钟的分析可以促进紧急治疗决策。